HRP20160562T1 - Derivat pirimidina kao inhibitori fak - Google Patents

Derivat pirimidina kao inhibitori fak Download PDF

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Publication number
HRP20160562T1
HRP20160562T1 HRP20160562TT HRP20160562T HRP20160562T1 HR P20160562 T1 HRP20160562 T1 HR P20160562T1 HR P20160562T T HRP20160562T T HR P20160562TT HR P20160562 T HRP20160562 T HR P20160562T HR P20160562 T1 HRP20160562 T1 HR P20160562T1
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Croatia
Prior art keywords
diseases
tautomers
stereoisomers
proportions
mixtures
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HRP20160562TT
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English (en)
Croatian (hr)
Inventor
Timo Heinrich
Christina Esdar
Hartmut Greiner
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Merck Patent Gmbh
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Publication of HRP20160562T1 publication Critical patent/HRP20160562T1/hr

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
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    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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    • A61P35/00Antineoplastic agents
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    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/88Nitrogen atoms, e.g. allantoin
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
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  • Chemical & Material Sciences (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Biomedical Technology (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Neurosurgery (AREA)
  • Urology & Nephrology (AREA)
  • Neurology (AREA)
  • Cardiology (AREA)
  • Obesity (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Oncology (AREA)
  • Hospice & Palliative Care (AREA)
  • Vascular Medicine (AREA)
  • Psychiatry (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
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  • Transplantation (AREA)
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HRP20160562TT 2010-08-18 2016-05-24 Derivat pirimidina kao inhibitori fak HRP20160562T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE102010034699A DE102010034699A1 (de) 2010-08-18 2010-08-18 Pyrimidinderivate
EP11743438.1A EP2606034B1 (fr) 2010-08-18 2011-07-19 Derivates de pyrimidine comme inhibiteurs de fak
PCT/EP2011/003597 WO2012022408A1 (fr) 2010-08-18 2011-07-19 Dérivés de pyrimidine en tant qu'inhibiteurs de fak

Publications (1)

Publication Number Publication Date
HRP20160562T1 true HRP20160562T1 (hr) 2016-06-17

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ID=44504442

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20160562TT HRP20160562T1 (hr) 2010-08-18 2016-05-24 Derivat pirimidina kao inhibitori fak

Country Status (17)

Country Link
US (1) US8906916B2 (fr)
EP (1) EP2606034B1 (fr)
JP (2) JP6049617B2 (fr)
CN (1) CN103052627B (fr)
AR (1) AR082722A1 (fr)
AU (1) AU2011291110B2 (fr)
CA (1) CA2808540C (fr)
DE (1) DE102010034699A1 (fr)
DK (1) DK2606034T3 (fr)
ES (1) ES2572740T3 (fr)
HR (1) HRP20160562T1 (fr)
HU (1) HUE027846T2 (fr)
IL (1) IL224751A (fr)
PL (1) PL2606034T3 (fr)
RS (1) RS54882B1 (fr)
SI (1) SI2606034T1 (fr)
WO (1) WO2012022408A1 (fr)

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DE102010034699A1 (de) * 2010-08-18 2012-02-23 Merck Patent Gmbh Pyrimidinderivate
CA2827171C (fr) * 2011-02-17 2019-04-09 Cancer Therapeutics Crc Pty Limited Inhibiteurs de fak
CA2827172C (fr) * 2011-02-17 2019-02-26 Cancer Therapeutics Crc Pty Limited Inhibiteurs selectifs de fak
US9013997B2 (en) 2012-06-01 2015-04-21 Broadcom Corporation System for performing distributed data cut-through
WO2014027199A1 (fr) * 2012-08-14 2014-02-20 Cancer Therapeutics Crc Pty Ltd Inhibiteurs de fak et flt3
US20160009686A1 (en) 2012-08-17 2016-01-14 Cancer Therapeutics Crc Pty Limited Vegfr3 inhibitors
US20150225377A1 (en) * 2012-08-17 2015-08-13 Cancer Therapeutics Crc Pty Limited Vegfr3 inhibitors
TW201412740A (zh) * 2012-09-20 2014-04-01 Bayer Pharma AG 經取代之吡咯并嘧啶胺基苯并噻唑酮
JPWO2014174745A1 (ja) * 2013-04-26 2017-02-23 国立大学法人京都大学 Eg5阻害剤
US10106834B2 (en) 2013-10-09 2018-10-23 The General Hospital Corporation Methods of diagnosing and treating B cell acute lymphoblastic leukemia
WO2015123722A1 (fr) * 2014-02-19 2015-08-27 Bionomics Limited Inhibiteurs
JP6684780B2 (ja) 2014-08-25 2020-04-22 ソーク インスティテュート フォー バイオロジカル スタディーズ 新規ulk1阻害剤およびそれを使用する方法
WO2019117813A1 (fr) * 2017-12-15 2019-06-20 National University Of Singapore Agents thérapeutiques ciblant une kinase d'adhésion focale pour le traitement du glaucome et de la fibrose

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AU2003224257A1 (en) 2002-04-09 2003-10-27 Astex Technology Limited Heterocyclic compounds and their use as modulators of p38 map kinase
EP1625121B1 (fr) 2002-12-20 2010-02-24 Pfizer Products Inc. Derives de pyrimidine destines au traitement de la croissance cellulaire anormale
UA80767C2 (en) * 2002-12-20 2007-10-25 Pfizer Prod Inc Pyrimidine derivatives for the treatment of abnormal cell growth
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AR082722A1 (es) 2012-12-26
IL224751A (en) 2015-03-31
US20130158005A1 (en) 2013-06-20
DK2606034T3 (en) 2016-05-02
DE102010034699A1 (de) 2012-02-23
SI2606034T1 (sl) 2016-07-29
JP6441861B2 (ja) 2018-12-19
JP2017036268A (ja) 2017-02-16
CA2808540C (fr) 2018-09-11
US8906916B2 (en) 2014-12-09
JP2013534227A (ja) 2013-09-02
EP2606034B1 (fr) 2016-03-09
ES2572740T3 (es) 2016-06-02
CA2808540A1 (fr) 2012-02-23
AU2011291110A1 (en) 2013-04-04
CN103052627A (zh) 2013-04-17
EP2606034A1 (fr) 2013-06-26
JP6049617B2 (ja) 2016-12-21
CN103052627B (zh) 2015-08-19
HUE027846T2 (en) 2016-11-28
WO2012022408A1 (fr) 2012-02-23

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